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Peer-reviewed veterinary case report

New blood test for detecting Chagas disease in dogs

By Fontes, Natália Dantas et al.·Published in Parasites & vectors·2024·alo Moniz Institute, Brazil·View original on PubMed

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Original publication title: Evaluation of chimeric recombinant antigens for the serodiagnosis of Trypanosoma cruzi in dogs: a promising tool for Chagas disease surveillance.

Species:
dog

Plain-English summary

A study evaluated new tests for detecting Chagas disease in dogs, which is caused by a parasite called Trypanosoma cruzi. Researchers tested 663 dog blood samples using four different antigens and found that two of them, IBMP-8.2 and IBMP-8.4, were particularly effective at identifying the disease. IBMP-8.2 had a sensitivity of nearly 90%, meaning it correctly identified most infected dogs, while IBMP-8.4 had a specificity of 98.6%, meaning it rarely gave false positives. These findings suggest that these tests could improve how we diagnose Chagas disease in dogs and help protect both canine and human health.

People also search for: dog Chagas disease symptoms · how to test dog for Trypanosoma cruzi · Chagas disease treatment for dogs

Abstract

BACKGROUND: Chagas disease (CD), a neglected parasitic disease caused by Trypanosoma cruzi, poses a significant health threat in Latin America and has emerged globally because of human migration. Trypanosoma cruzi infects humans and over 100 other mammalian species, including dogs, which are important sentinels for assessing the risk of human infection. Nonetheless, the serodiagnosis of T. cruzi in dogs is still impaired by the absence of commercial tests. In this study, we investigated the diagnostic accuracy of four chimeric recombinant T. cruzi IBMP antigens (IBMP-8.1, IBMP-8.2, IBMP-8.3, and IBMP-8.4) for detecting anti-T. cruzi antibodies in dogs, using latent class analysis (LCA). METHODS: We examined 663 canine serum samples, employing indirect ELISA with the chimeric antigens. LCA was utilized to establish a latent variable as a gold standard for T. cruzi infection, revealing distinct response patterns for each antigen. RESULTS: The IBMP (Portuguese acronym for the Molecular Biology Institute of Paraná) antigens achieved area under the ROC curve (AUC) values ranging from 90.9% to 97.3%. The highest sensitivity was attributed to IBMP-8.2 (89.8%), while IBMP-8.1, IBMP-8.3, and IBMP-8.4 achieved 73.5%, 79.6%, and 85.7%, respectively. The highest specificity was observed for IBMP-8.4 (98.6%), followed by IBMP-8.2, IBMP-8.3, and IBMP-8.1 with specificities of 98.3%, 94.4%, and 92.7%, respectively. Predictive values varied according to prevalence, indicating higher effectiveness in endemic settings. CONCLUSIONS: Our findings underscore the remarkable diagnostic performance of IBMP-8.2 and IBMP-8.4 for the serodiagnosis of Trypanosoma cruzi in dogs, representing a promising tool for the diagnosis of CD in dogs. These chimeric recombinant antigens may not only enhance CD surveillance strategies but also hold broader implications for public health, contributing to the global fight against this neglected tropical disease.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39010122/